US6485929B1 - Method for inhibiting CD95-independent apoptosis in AIDS - Google Patents

Method for inhibiting CD95-independent apoptosis in AIDS Download PDF

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US6485929B1
US6485929B1 US09/600,522 US60052200A US6485929B1 US 6485929 B1 US6485929 B1 US 6485929B1 US 60052200 A US60052200 A US 60052200A US 6485929 B1 US6485929 B1 US 6485929B1
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cxcr4
bonding
cells
hiv
factor
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Peter Krammer
Christina Berndt
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Deutsches Krebsforschungszentrum DKFZ
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2803—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily
    • C07K16/2812—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against the immunoglobulin superfamily against CD4
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A61P31/18—Antivirals for RNA viruses for HIV
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/04—Immunostimulants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/52—Cytokines; Lymphokines; Interferons
    • C07K14/521—Chemokines
    • C07K14/522—Alpha-chemokines, e.g. NAP-2, ENA-78, GRO-alpha/MGSA/NAP-3, GRO-beta/MIP-2alpha, GRO-gamma/MIP-2beta, IP-10, GCP-2, MIG, PBSF, PF-4, KC
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
    • C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
    • C07K14/705—Receptors; Cell surface antigens; Cell surface determinants
    • C07K14/70503—Immunoglobulin superfamily
    • C07K14/70539—MHC-molecules, e.g. HLA-molecules
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/28—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants
    • C07K16/2866—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against receptors, cell surface antigens or cell surface determinants against receptors for cytokines, lymphokines, interferons
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides

Abstract

The invention relates to a method for inhibiting CD95-independent apoptosis, comprising the following steps:
(a) blocking the bonding of HIV-1 gp120 on receptors CD4 and/or CXCR4 or of a factor competing for this bonding, and/or
(b) inhibiting the signal path induced by the bonding of (a).
The invention also relates to a system for identifying substances which can be utilized for inhibiting CD95-independent apoptosis.

Description

FIELD OF THE INVENTION
The present invention relates to a method of inhibiting CD95-independent apoptosis, in particular in the case of AIDS. The invention also relates to a system for identifying substances which can be used for inhibiting CD95-independent apoptosis.
BACKGROUND OF THE INVENTION
AIDS is characterized by a depletion of CD4+T cells and a dysfunction of the immune system. Previous data refer to the fact that a depletion occurs because the CD95 receptor is activated by the CD95 ligand present in increased amount in the presence of the glycoprotein gp120 of HIV, so that apoptosis, i.e. programmed cell death, is induced in CD4+T cells. This apoptosis is referred to as CD95-mediated apoptosis.
Experiments have been made to prevent the depletion of CD4+T cells in the case of AIDS. For this purpose, methods were carried out with substances which block the bonding of the CD95 ligand to the CD95 receptor. However, these methods did not fully prevent the depletion of CD4+T cells.
Therefore, it is the object of the present invention to provide a method by which the depletion of CD4+T cells in the case of AIDS can be investigated and optionally be prevented.
According to the invention this is achieved by the subject matters defined in the claims.
SUMMARY OF THE INVENTION
The subject matter of the present invention relates to a method of inhibiting CD95-independent apoptosis, the method comprising the steps of:
(a) blocking the bonding of HIV-1 gp120 to receptors CD4 and/or CXCR4 and blocking a factor competing for this bonding, respectively, and/or
(b) inhibiting the signal path induced by the bonding of (a).
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 shows the percent of cell death of HPB-ALL cells when incubated with anti-CD4 antibody or CXCR4 antibody.
FIG. 2 shows the percent of specific cell death of BJAB cells, which express CD4, CXCR4 or CD4 and CXCR4.
FIG. 3 shows the percent of specific cell death when incubated with anti-CXCR4 antibody.
DETAILED DESCRIPTION OF THE INVENTION
The present invention is based on the applicant's insight that not only CD95-mediated apoptosis but also CD95-independent apoptosis may occur in cells. He found that the CD95-independent apoptosis is induced e.g. in that the glycoprotein gp120 of HIV-1 binds to the receptors CD4 and/or CXCR4. These receptors are present in different cells. The applicant also realized that the receptors CD4 and CXCR4 can also be activated by other factors through which apoptosis is induced. These factors are in particular those competing with HIV-1 gp120 for the bonding to receptors CD4 and CXCR4. Furthermore, the applicant found that the CD95-independent apoptosis differs from the CD95-mediated apoptosis as regards various properties. Some of these properties are listed in below Table 1.
TABLE 1
CD95- CD95-
CD95- independent independent
mediated apoptosis apoptosis
apoptosis via CD4 via CXCR4
DNA breakdown + − −
Kinetics ˜12 H ˜15 min ˜15 min
Changes in FSC/SSC + + +
Loss of membrane asymmetry + + +
Chromatin condensation + + +
ΔΨm + + +
7-AAD-test positive+) + + ND*)
Inhibition by zVAD-fmk + − −
Caspase-3 cleavage + − −
Caspase-8 cleavage + − −
PARP cleavage + − −
+)Apoptotic cells can be differentiated from necrotic cells by staining using the fluorescent dye 7-amino-actinomycin D (7-AAD).
*)not determined
According to the invention the above insights are used for a method by which CD95-independent apoptosis can be inhibited. Such a method comprises the steps of:
(a) blocking the bonding of HIV-1 gp120 to receptors CD4 and/or CXCR4 and blocking a factor competing for this bonding, respectively, and/or
(b) inhibiting the signal path induced by the bonding of (a).
The expression “receptors CD4 and/or CXCR4” refers to the fact that these receptors can be present in cells of any kind and origin. In particular, these may be cells in which CD4 and/or CXCR4 occur by nature. Examples of such cells are CD4+/CXCR4+T cells, such as HPB-ALL cells. The cells may also be cells in which CD4 and/or CXCR4 does not occur by nature but which have been introduced artificially. Examples of such cells are lymphoblastoid B cells, such as BJAB cells. Furthermore, the expression “receptors CD4 and/or CXCR4” also comprises those portions of these receptors to which HIV-1 gp120 or a factor competing therewith can bind.
The expression “a factor competing for the bonding” comprises any factor which can compete with HIV-1 gp120 for the bonding to receptors CD4 and/or CXCR4. In particular, the factor may be an anti-CD4 antibody, such as HP2/6 (Carrera, University of Madrid) or IOT4A (Immunotech). The factor may also be an anti-CXCR4 antibody, such as 12G5 (R+D Systems). Moreover, the factor may be another HIV protein, e.g. the glycoprotein gp160. An above HIV protein may originate from any HIV strain, in particular from HIV-1 or HIV-2. Furthermore, the factor may be a protein which is derived from a HIV protein. Such a protein can comprise e.g. the region responsible in HIV proteins for the binding to the receptors CD4 and CXCR4.
The expression “blocking the bonding” comprises any kind and any means by which the bonding of HIV-1 gp120 to receptors CD4 and/or CXCR4 and a factor competing for this bonding, respectively, can be blocked. In particular, the means can be the natural ligand of CD4, such as an MHC molecule. The means can also be the natural ligand of CXCR4, such as SDF-1α. It may be favorable for the natural ligands of CD4 and CXCR4 to be used jointly.
The expression “inhibition of the signal path” comprises any kind and any means by which the signal path can be inhibited, which is induced by the bonding of HIV-1 gp120 to the receptors CD4 and/or CXCR4 and a factor competing for this bonding, respectively. In particular, the means may be one by which the loss of membrane asymmetry can be prevented. The means may also be one by which the condensation of chromatin can be prevented.
According to the invention there is also provided a system by which CD95-independent apoptosis can be investigated. Furthermore, substances can be identified by this system, which are suitable for the inhibition of CD95-independent apoptosis. Such a system comprises cells which are CD4+ and/or CXCR4+, and HIV-1 gp120 and a factor which competes with HIV-1 gp120 for the bonding to CD4+ and/or CXCR4+, respectively, as well as optionally a substance whose inhibitory effect shall be determined on the bonding of HIV-1 gp120 to the receptors CD4 and/or CXCR4 or a factor competing for this bonding and on the signal path induced by this binding, respectively. It may be favorable for the system to also contain a substance whose inhibitory effect is known. The above statements apply correspondingly to such substances as well as other components of the system.
By means of the present invention it is possible to investigate and influence CD95-independent apoptosis. In particular, it is possible to inhibit CD95-independent apoptosis. On the other hand, the invention also refers to the possiblities of inducing CD95-independent apoptosis. Such possibilities will result inter alia from the use of factors which compete with the bonding of HIV-1 gp120 to receptors CD4 and/or CXCR4. Such factors are in particular antibodies directed against CD4 and CXCR4, respectively. Furthermore, the present invention enables to identify substances which can influence, in particular inhibit, CD95-independent apoptosis.
Therefore, the present invention represents the possibility of inhibiting and inducing, respectively, CD95-independent apoptosis. Thus, the present invention provides a means for preventing the depletion of CD4+T cells in the case of AIDS. Furthermore, the present invention represents a means for inducing CD95-independent apoptosis in well-calculated fashion, which is of significance in particular for combating tumor cells.
EXAMPLES
The invention is explained by the below example.
Example
Induction of CD95-independent Apoptosis and its Inhibition
I. Induction of CD95-independent Apoptosis
(a) CD4+/CXCR4+ cells (HPB-ALL cells) are used. HPB-ALL cells are CD95−, i.e. no CD95-mediated apoptosis occurs in them.
1×105 HPB-ALL cells are incubated with 5 μg/ml mouse anti-CD4 antibody (HP2/6) and mouse anti CXCR4 antibody (12G5), respectively, at 37° C. for 15 minutes. Then, the bound antibodies are reacted with sheep anti-mouse antibodies (100 μg/ml, Boehringer). Apoptosis detection is carried out in which an FSC/SSC analysis is run in an FACScan cytometer at various times (cf. FIG. 1).
It shows that the antibodies anti-CD4 and anti-CXCR4, respectively, can each induce CD95-independent apoptosis.
(b) CD4−/CXCR4− cells (BJAB cells) are used. The receptors CD4 and CXCR4 are introduced into these cells by transfecting DNA constructs coding for the receptors into the cells and then expressing them.
BJAB cells are transfected with 2 μg of the hygromycin resistance vector pKEX2XL and 10 μg of the vector pCDM8-CD4 (Kolanus, University of Munich). Cell clones are selected in the presence of hygromycin B (450 U/ml). Select cell clones and BJAB cells, respectively, are also transfected with 10 μg of the vector pcDNA3-tag-CXCR4 (Moulard, University of Marseille). Cell clones are selected in the presence of G418 (4 mg/ml). Select cell clones of both transfection cycles are tested for the expression of the corresponding receptors. Cell clones which express CD4, CXCR4 or CD4 and CXCR4, are subjected to an apoptosis induction as described under (a) (cf. FIG. 2).
It shows that CD95-independent apoptosis can be induced in cells into which CD4 and/or CXCR4 has been introduced artificially.
II. Inhibition of CD95-independent Apoptosis
HPB-ALL cells are incubated with 250 nM SDF-1α at 37° C. for 30 minutes. The cells are then subjected to an apoptosis induction using the mouse anti-CXCR4 antibody (12G5), as described above under item I. (a).
It shows that the induction of cd95-independent apoptosis can be prevented by means of the artificial ligand of cxcr4, SDF-1α.

Claims (10)

What is claimed is:
1. A method of inhibiting CD95-independent apoptosis, comprising the steps of:
(a) blocking the bonding of HIV-1 gp120 to receptors CD4 and/or with a competing factor for said bonding, and/or
(b) inhibiting the signal path induced by the bonding of (a).
2. The method according to claim 1, wherein the competing factor is an anti-CD4 antibody.
3. The method according to claim 1, wherein the competing factor is an anti-CXCR4 antibody.
4. The method according to any one of claims 1 to 3, wherein (a) is blocked by a natural ligand of CD4 and/or a natural ligand of CXCR4.
5. The method of claim 4, wherein the natural ligand of CD4 is an MHC molecule.
6. The method according to claim 4, wherein the natural ligand of CXCR4 is SDF-1α.
7. A system for identifying substances suitable to inhibit CD95-independent apoptosis, comprising CD4+ and/or CXCR4+ cells, HIV-1 gp120, and a factor competing with HIV-1 gp120 for the bonding to CD4+ and/or CXCR4+.
8. The system according to claim 7, wherein the inhibitory effect of said factor is determined on the bonding of HIV-1 gp120 to receptors CD4 and/or CXCR4 or on the signal path induced by this bonding.
9. The system according to claim 7 or 8, wherein the factor is an anti-CD4 antibody.
10. The system according to claim 7 or 8, wherein the factor is an anti-CXCR4 antibody.
US09/600,522 1998-01-15 1999-01-15 Method for inhibiting CD95-independent apoptosis in AIDS Expired - Fee Related US6485929B1 (en)

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DE19801265A DE19801265C1 (en) 1998-01-15 1998-01-15 Inhibition of CD95-independent apoptosis in AIDS
DE19801265 1998-01-15
PCT/DE1999/000109 WO1999036091A2 (en) 1998-01-15 1999-01-15 Method for inhibiting cd95-independent apoptosis in aids

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060000038A1 (en) * 2002-09-27 2006-01-05 Gatzemeyer John J Brush section for a powered toothbrush
WO2010127166A2 (en) 2009-04-30 2010-11-04 The Regents Of The University Of California Combination anti-hiv vectors, targeting vectors, and methods of use
WO2014026053A1 (en) 2012-08-09 2014-02-13 The Regents Of The University Of California Cd25 pre-selective combination anti-hiv vectors, targeting vectors, and methods of use
US8748107B2 (en) 2010-02-10 2014-06-10 Affitech Research As Isolated antibodies which bind to CXC chemokine receptor 4

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2265701A (en) * 1999-12-16 2001-06-25 Tanox, Inc. Anti-hiv-1 conjugates for treatment of hiv disease
WO2007049771A1 (en) 2005-10-28 2007-05-03 Ono Pharmaceutical Co., Ltd. Compound containing basic group and use thereof
ES2407115T3 (en) 2005-11-18 2013-06-11 Ono Pharmaceutical Co., Ltd. Compound containing a basic group and its use
EP2297206A1 (en) * 2008-05-14 2011-03-23 Eli Lilly And Company Anti-cxcr4 antibodies
WO2010043650A2 (en) * 2008-10-14 2010-04-22 Ablynx Nv Amino acid sequences directed against cellular receptors for viruses and bacteria

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
Berndt, C. et al., "CXCR4 and CD4 Mediate A Rapid CD95-Independent Cell Death In CD4+T Cells", Proceedings of the National Academy of Sciences of USA, 95:12556-12561, (Oct., 1998).
Corbeil, J. and Reichman, D.D., "Productive Infection and Subsequent Interaction of CD4+T Cells", Journal of General Virology, 76:681-690, (1995).
Radrizzani, et al., "IL-12 Inhibits Apoptosis Induced In A Human Th1 Clone By gp120/CD4 Cross-Linking and CD3/TCR Activation or By IL-2 Deprivation", Cell. Immunol., 161:14-21 (Mar., 1995).

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20060000038A1 (en) * 2002-09-27 2006-01-05 Gatzemeyer John J Brush section for a powered toothbrush
WO2010127166A2 (en) 2009-04-30 2010-11-04 The Regents Of The University Of California Combination anti-hiv vectors, targeting vectors, and methods of use
US8748107B2 (en) 2010-02-10 2014-06-10 Affitech Research As Isolated antibodies which bind to CXC chemokine receptor 4
US9353185B2 (en) 2010-02-10 2016-05-31 Affitech Research As Antibodies
WO2014026053A1 (en) 2012-08-09 2014-02-13 The Regents Of The University Of California Cd25 pre-selective combination anti-hiv vectors, targeting vectors, and methods of use

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DE19801265C1 (en) 1999-08-12
DE59902180D1 (en) 2002-09-05
ATE221389T1 (en) 2002-08-15
WO1999036091A3 (en) 1999-09-16
JP2002509118A (en) 2002-03-26
WO1999036091A2 (en) 1999-07-22

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